Variant report

Variant	esv3339485
Chromosome Location	chr6:71665256-71667804
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:854)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:71665724-71665822	K562	blood:	n/a	n/a
2	BACH1	chr6:71666632-71667239	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:71665197-71665977	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr6:71665562-71665959	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:71665543-71665974	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:71665559-71665903	A549	lung:	n/a	n/a
7	BHLHE40	chr6:71665561-71665878	HepG2	liver:	n/a	n/a
8	BHLHE40	chr6:71665506-71665972	K562	blood:	n/a	n/a
9	BHLHE40	chr6:71665473-71666207	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:71665497-71666133	GM12878	blood:	n/a	n/a
11	BRCA1	chr6:71665698-71665952	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr6:71665685-71665822	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr6:71665615-71665884	K562	blood:	n/a	n/a
14	CCNT2	chr6:71665587-71665988	K562	blood:	n/a	n/a
15	CEBPB	chr6:71665743-71665911	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:71665684-71665939	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr6:71665757-71665937	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr6:71665649-71665913	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr6:71666550-71666719	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr6:71665637-71665917	GM12878	blood:	n/a	n/a
21	CHD2	chr6:71665731-71665861	K562	blood:	n/a	n/a
22	CHD2	chr6:71665706-71665943	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr6:71665713-71666062	HepG2	liver:	n/a	n/a
24	CREB1	chr6:71665490-71665940	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr6:71665597-71665994	A549	lung:	n/a	n/a
26	CTBP2	chr6:71665240-71667308	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr6:71665700-71665850	SAEC	small airway:	n/a	n/a
28	CTCF	chr6:71665565-71665987	GM12892	blood:	n/a	n/a
29	CTCF	chr6:71665644-71665971	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr6:71665720-71665870	GM12868	blood:	n/a	n/a
31	CTCF	chr6:71665800-71665950	WI-38	lung:	n/a	n/a
32	CTCF	chr6:71665740-71665890	GM12866	blood:	n/a	n/a
33	CTCF	chr6:71665352-71665357	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:71665537-71665992	T-47D	breast:	n/a	n/a
35	CTCF	chr6:71665541-71665952	HepG2	liver:	n/a	n/a
36	CTCF	chr6:71665720-71665870	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:71665619-71665959	GM13977	blood:	n/a	n/a
38	CTCF	chr6:71665626-71665907	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr6:71665760-71665910	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr6:71666600-71666750	HVMF	connective:	n/a	n/a
41	CTCF	chr6:71665740-71665890	NHEK	skin:	n/a	n/a
42	CTCF	chr6:71665720-71665870	GM12867	blood:	n/a	n/a
43	CTCF	chr6:71665700-71665850	HCM	heart:	n/a	n/a
44	CTCF	chr6:71665740-71665890	HAc	cerebellar:	n/a	n/a
45	CTCF	chr6:71665563-71665973	A549	lung:	n/a	n/a
46	CTCF	chr6:71665638-71665942	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr6:71665740-71665890	HRE	kidney:	n/a	n/a
48	CTCF	chr6:71665547-71665980	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:71665740-71665890	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr6:71665720-71665870	RPTEC	kidney:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:71666803-71666853	BE2_C	brain:	n/a
2	chr6:71665936-71665986	ProgFib	skin:	n/a
3	chr6:71666809-71666859	HCF	heart:	n/a
4	chr6:71667105-71667155	PFSK-1	brain:	n/a
5	chr6:71667105-71667155	HIPEpiC	eye:	n/a
6	chr6:71666121-71666171	GM19239	blood:	n/a
7	chr6:71667105-71667155	BE2_C	brain:	n/a
8	chr6:71666858-71666908	HUVEC	blood vessel:	n/a
9	chr6:71666121-71666171	MCF-7	breast:	n/a
10	chr6:71666282-71666332	NT2-D1	testis:	n/a
11	chr6:71665936-71665986	HCPEpiC	choroid plexus:	n/a
12	chr6:71665395-71665445	NH-A	brain:	n/a
13	chr6:71665574-71665624	HCPEpiC	choroid plexus:	n/a
14	chr6:71666682-71666732	SKMC	muscle:	n/a
15	chr6:71667067-71667117	HEK293	kidney:	embryo
16	chr6:71666063-71666113	ovcar-3	ovarian:	n/a
17	chr6:71665395-71665445	IMR90	lung:	fetal
18	chr6:71666121-71666171	HEEpiC	esophagus:	n/a
19	chr6:71666121-71666171	Hela-S3	cervix:	n/a
20	chr6:71666682-71666732	AoSMC	blood vessel:	n/a
21	chr6:71667105-71667155	PrEC	prostate:	n/a
22	chr6:71666803-71666853	RPTEC	kidney:	n/a
23	chr6:71666121-71666171	K562	blood:	n/a
24	chr6:71666063-71666113	NHBE	bronchial:	n/a
25	chr6:71665574-71665624	SK-N-SH_RA	brain:	n/a
26	chr6:71666803-71666853	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:71666682-71666732	AG04449	skin:	fetal
28	chr6:71665574-71665624	ECC-1	luminal epithelium:	n/a
29	chr6:71666824-71666874	HEK293	kidney:	embryo
30	chr6:71666682-71666732	SK-N-MC	brain:	n/a
31	chr6:71666282-71666332	Hepatocyte	liver:	n/a
32	chr6:71666824-71666874	GM06990	blood:	n/a
33	chr6:71665936-71665986	HepG2	liver:	n/a
34	chr6:71667105-71667155	HepG2	liver:	n/a
35	chr6:71666063-71666113	A549	lung:	n/a
36	chr6:71666282-71666332	IMR90	lung:	fetal
37	chr6:71666858-71666908	H1-hESC	embryonic stem cell:	embryo
38	chr6:71666824-71666874	NHBE	bronchial:	n/a
39	chr6:71666282-71666332	Hela-S3	cervix:	n/a
40	chr6:71666682-71666732	CMK	blood:	n/a
41	chr6:71666824-71666874	PrEC	prostate:	n/a
42	chr6:71665522-71665572	GM12892	blood:	n/a
43	chr6:71666282-71666332	HCM	heart:	n/a
44	chr6:71667067-71667117	Caco-2	colon:	n/a
45	chr6:71666809-71666859	GM19239	blood:	n/a
46	chr6:71666282-71666332	RPTEC	kidney:	n/a
47	chr6:71666282-71666332	BE2_C	brain:	n/a
48	chr6:71666803-71666853	HEK293	kidney:	embryo
49	chr6:71666809-71666859	HCM	heart:	n/a
50	chr6:71665574-71665624	HNPCEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:71230031..71231237-chr6:71665008..71666316,7	MCF-7	breast:
2	chr6:71416313..71416967-chr6:71665219..71666338,4	MCF-7	breast:
3	chr6:71415956..71416839-chr6:71665369..71665919,2	K562	blood:
4	chr6:71415810..71416633-chr6:71665559..71666663,3	MCF-7	breast:
5	chr6:71256857..71257781-chr6:71665609..71666111,2	MCF-7	breast:
6	chr6:71594169..71594842-chr6:71665262..71666233,2	MCF-7	breast:

No data

Variant related genes	Relation type
B3GAT2	TF binding region
B3GAT2	CpG island

Extended variants
information (count: 99 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575034145	chr6:71665288-71665289	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542393072	chr6:71665342-71665343	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554413887	chr6:71665349-71665350	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs572740654	chr6:71665381-71665382	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546496162	chr6:71665400-71665401	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564663492	chr6:71665443-71665444	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532126324	chr6:71665472-71665473	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9455275	chr6:71665473-71665474	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs62420336	chr6:71665479-71665480	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs529749468	chr6:71665490-71665491	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200162847	chr6:71665680-71665681	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373530810	chr6:71665725-71665726	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149577161	chr6:71665731-71665732	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527522804	chr6:71665734-71665735	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112409269	chr6:71665735-71665736	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370336662	chr6:71665751-71665752	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs552429904	chr6:71665758-71665759	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373218616	chr6:71665759-71665760	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs199757620	chr6:71665776-71665777	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143511495	chr6:71665782-71665783	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376563227	chr6:71665790-71665791	Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9446312	chr6:71665851-71665852	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs369211351	chr6:71665857-71665858	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372158787	chr6:71665858-71665859	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534598813	chr6:71665862-71665863	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201430647	chr6:71665865-71665866	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147151504	chr6:71665875-71665876	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556286650	chr6:71665889-71665890	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568523673	chr6:71665913-71665914	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199861185	chr6:71665950-71665951	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535966421	chr6:71665952-71665953	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554377076	chr6:71665976-71665977	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200678168	chr6:71665982-71665983	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1574490	chr6:71665986-71665987	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs143347651	chr6:71666037-71666038	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576680331	chr6:71666105-71666106	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1320315	chr6:71666146-71666147	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371411394	chr6:71666154-71666155	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562160390	chr6:71666214-71666215	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9446313	chr6:71666227-71666228	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs377152159	chr6:71666258-71666259	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559736877	chr6:71666277-71666278	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs34685178	chr6:71666332-71666333	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs559849290	chr6:71666333-71666334	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527470688	chr6:71666344-71666345	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370250434	chr6:71666379-71666380	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs552134267	chr6:71666402-71666403	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569875120	chr6:71666424-71666425	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs564359077	chr6:71666442-71666443	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535666593	chr6:71666468-71666469	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71663400-71665800	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
2	chr6:71663600-71667000	Active TSS	Brain Cingulate Gyrus	brain
3	chr6:71663800-71667200	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr6:71663800-71667600	Active TSS	Brain Anterior Caudate	brain
5	chr6:71664200-71667600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
6	chr6:71664600-71667000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
7	chr6:71664600-71667400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
8	chr6:71664800-71665400	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr6:71664800-71665400	Bivalent Enhancer	Fetal Heart	heart
10	chr6:71664800-71665400	Bivalent Enhancer	Fetal Lung	lung
11	chr6:71664800-71666000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
12	chr6:71664800-71666800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
13	chr6:71664800-71667200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
14	chr6:71664800-71667400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
15	chr6:71664800-71667400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
16	chr6:71664800-71667800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr6:71665000-71665400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
18	chr6:71665000-71665400	Bivalent Enhancer	Fetal Brain Male	brain
19	chr6:71665000-71666200	Active TSS	H9 Cell Line	embryonic stem cell
20	chr6:71665000-71667000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
21	chr6:71665000-71667000	Active TSS	Fetal Brain Female	brain
22	chr6:71665000-71667400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:71665000-71667600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
24	chr6:71665000-71667600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
25	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:71665200-71665400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:71665200-71665400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr6:71665200-71665400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
32	chr6:71665200-71665400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
33	chr6:71665200-71665400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
34	chr6:71665200-71665400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
35	chr6:71665200-71665400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:71665200-71665400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:71665200-71665400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr6:71665200-71665400	Flanking Active TSS	Aorta	Aorta
39	chr6:71665200-71665400	Flanking Active TSS	Brain Substantia Nigra	brain
40	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
41	chr6:71665200-71665400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
42	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
43	chr6:71665200-71665400	Bivalent/Poised TSS	Fetal Kidney	kidney
44	chr6:71665200-71665400	Bivalent Enhancer	Placenta	Placenta
45	chr6:71665200-71665400	Enhancers	Lung	lung
46	chr6:71665200-71665400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
47	chr6:71665200-71665400	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
48	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
49	chr6:71665200-71665400	Bivalent Enhancer	Spleen	Spleen
50	chr6:71665200-71665400	Flanking Bivalent TSS/Enh	GM12878-XiMat	blood

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